CN112812379B - Degradable film and preparation method thereof - Google Patents
Degradable film and preparation method thereof Download PDFInfo
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- CN112812379B CN112812379B CN202110166152.9A CN202110166152A CN112812379B CN 112812379 B CN112812379 B CN 112812379B CN 202110166152 A CN202110166152 A CN 202110166152A CN 112812379 B CN112812379 B CN 112812379B
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2305/00—Characterised by the use of polysaccharides or of their derivatives not provided for in groups C08J2301/00 or C08J2303/00
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2401/00—Characterised by the use of cellulose, modified cellulose or cellulose derivatives
- C08J2401/08—Cellulose derivatives
- C08J2401/26—Cellulose ethers
- C08J2401/28—Alkyl ethers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2405/00—Characterised by the use of polysaccharides or of their derivatives not provided for in groups C08J2401/00 or C08J2403/00
- C08J2405/08—Chitin; Chondroitin sulfate; Hyaluronic acid; Derivatives thereof
Abstract
The invention relates to the technical field of membrane materials, and provides a degradable membrane which comprises the following raw materials in parts by weight: 0.5-2 parts of gracilaria crispatus polysaccharide, 0.2-1 part of chitosan, 0.05-0.1 part of sodium carboxymethylcellulose, 0.5-3 parts of low-temperature co-melting solvent and 94-99 parts of distilled water. The invention takes the gracilaria polysaccharide, chitosan and sodium carboxymethylcellulose as raw materials, takes a low-temperature co-melting solvent as a dissolution promoter and a plasticizer and takes distilled water as a solvent, and the degradable film is obtained by heating and stirring the materials until the materials are colorless transparent liquid, pouring the liquid into a container, drying and uncovering the film. The degradable film prepared by the invention has wide raw material source, low cost, simple operation and degradability, so that the degradable polysaccharide film has wider application prospect, and the application fields and research directions of the fragile gracilaria polysaccharide and the low-temperature eutectic solvent are widened.
Description
Technical Field
The invention relates to the technical field of membrane materials, in particular to a degradable membrane based on gracilaria crispatus polysaccharide and a low-temperature eutectic solvent and a preparation method thereof.
Background
Synthetic plastics have been rapidly developed and spread throughout the life of people in the past decades with excellent properties and low cost, but since synthetic plastics are not degradable, serious pollution is caused to the environment, and research and development of degradable plastics are enhanced by many domestic enterprises. The degradable membrane materials are mainly divided into the following three types: the first kind of film made of light degradable material such as polylactic acid (PLA), acetate fiber (CA) etc. has the performance comparable to the traditional PVDF, PES film, but the degradation of this kind of film material needs certain illumination, temperature and humidity, and the time needed for degradation is longer; the second membrane material is of a biological destruction type, natural polymers such as starch, protein and sodium carboxymethyl cellulose are blended or monomer-copolymerized in a mixed dispersion system with synthetic polymers such as polyethylene and polypropylene, and the copolymer structure is destroyed through degradation of natural components; the third membrane material is biodegradable, is based on natural polymers or modified materials, and can be completely decomposed without residue.
At present, many researches are focused on degradable natural polymer synthetic membranes, and membrane materials with market prospects have good barrier properties and mechanical strength. The polysaccharide substance is cheap and easy to obtain, degradable, has good film forming property, and is widely applied to food, cosmetics, sewage industry, biomedical treatment and the like. However, films formed from polysaccharides alone are generally less stable, mechanically, water vapor barrier, and bacteriostatic than synthetic materials. A common method of improving the performance of polysaccharide films is to blend with other polymers or to add fillers, forming more complex structures through the interaction between the matrix and the filler. The crisp gracilaria is large-scale algae of gracilaria of gracilariaceae of Gigartinales of Rhodophyta, is widely cultivated in southeast of China along coast, has the characteristics of edible property, no toxicity, good water solubility, large viscosity and the like, has the activity of regulating immunity, resisting tumor and the like, and has no report on the application of the crisp gracilaria polysaccharide in the aspect of materials at present.
The low-temperature eutectic solvent (DES) is a novel green environment-friendly solvent which is rapidly developed in recent years, and is widely applied to chemical processes such as extraction, synthesis and the like. DES has thermal stability, high solubility, low melting point, and low price, easy availability, low toxicity or no toxicity, and is biodegradable. These characteristics make them very attractive for degradable film applications from a green environmental point of view. However, the current relevant research reports mainly focus on the aspects of preparing batteries by DES extractive distillation, dissolving cellulose, deposition and the like, and the application of DES in promoting polysaccharide dissolution or enhancing the mechanical properties of membrane materials is not reported for a while.
Therefore, how to provide a degradable film based on the gracilaria polysaccharide and a low temperature eutectic solvent is a problem to be solved urgently by those skilled in the art.
Disclosure of Invention
In view of the above, the invention provides a degradable film and a preparation method thereof, the degradable film has wide raw material sources, low cost, simple operation and degradability, so that the degradable polysaccharide film has wider application prospects, and the invention also widens the application fields and research directions of the gracilaria polysaccharide and the low-temperature eutectic solvent.
In order to achieve the purpose, the invention adopts the following technical scheme:
a degradable film comprises the following raw materials in parts by weight: 0.5-2 parts of gracilaria crispata polysaccharide, 0.2-1 part of chitosan, 0.05-0.1 part of sodium carboxymethylcellulose, 0.5-3 parts of low-temperature co-melting solvent and 98-110 parts of distilled water.
Preferably, in the degradable film, the low-temperature co-melting solvent is prepared from choline chloride, glycerol and lactic acid in a mass ratio of (1-3): (0.5-2): (0.5-2).
The beneficial effects of the above technical scheme are: compared with the prior art, the crisp gracilaria polysaccharide adopted by the invention takes materials which are eaten by people in daily life as raw materials, has higher viscosity and stronger coagulability, is easy to dissolve in water, and can enhance the mechanical strength of the packaging film; the film material can be used in the fields of packaging films of food and medicines, soil slow-release mulching films and the like.
Preferably, in the above degradable membrane, the molecular weight of the gracilaria polysaccharide is greater than 200 kDa.
The beneficial effects of the above technical scheme are: the gracilaria polysaccharide with larger molecular weight has high viscosity and stronger coagulability, and is easier to form a film material.
The invention also discloses a preparation method of the degradable membrane, which comprises the following steps: the method comprises the steps of taking gracilaria crispa polysaccharide, chitosan and sodium carboxymethylcellulose as raw materials, taking a low-temperature co-melting solvent formed by choline chloride, glycerol and lactic acid as a dissolution promoter and a plasticizer, taking distilled water as a solvent, heating and stirring until the solution is colorless and transparent, pouring the solution into a container, drying, and uncovering the film to obtain the degradable film.
The hydrogen bonds formed by the interaction among the hydroxyl in the sodium carboxymethyl cellulose, the hydroxyl and the amino in the chitosan and the hydroxyl in the gracilaria polysaccharide ensure that the bonding force in the film is tighter.
Preferably, in the above degradable film, the method comprises the following steps:
(1) weighing choline chloride, glycerol and lactic acid, and stirring under heating condition to obtain colorless transparent liquid, namely the low-temperature co-melting solvent;
(2) adding a small amount of low-temperature co-melting solvent into the fragile gracilaria polysaccharide, and dissolving in distilled water to obtain a fragile gracilaria solution;
(3) adding a small amount of low-temperature co-melting solvent into chitosan and sodium carboxymethyl cellulose, and dissolving in distilled water to obtain a chitosan and sodium carboxymethyl cellulose blending solution;
(4) pouring the chitosan and sodium carboxymethylcellulose blend into the gracilaria solution, stirring and mixing under heating to uniform state, then pouring into a container, drying, and uncovering the film to obtain the degradable film.
Preferably, in one of the above degradable films, the temperature of heating is 50 to 80 ℃.
The technical scheme has the beneficial effects that the polysaccharide-based degradable membrane material provided by the invention adopts a plurality of polysaccharides compounded in proportion as a matrix, and choline chloride, glycerol and lactic acid are added as plasticizers, so that the prepared degradable membrane has strong mechanical property and high transparency, is degradable in water, and can be applied to food packaging membranes, soil fertilizer slow-release mulching membranes and the like.
Preferably, in the degradable film, the drying is drying for 6-10h in a blast dryer at 40-70 ℃ until the film is formed.
The technical scheme has the beneficial effects that the film material obtained by drying at the temperature is relatively transparent and is easy to peel.
Preferably, in one of the degradable membranes, the mass ratio of the gracilaria polysaccharide, the low-temperature co-melting solvent and the distilled water in the step (2) is 1-2: 0.5-3: 50, more preferably 1: 0.5: 50.
the technical scheme has the beneficial effects that the gracilaria cilaria is a large-scale economic cultivation seaweed peculiar to China, is rich in various active polysaccharides, and has the activities of immunoregulation activity, antioxidation and the like. The polysaccharide mixed solution obtained in the proportion is uniform, has moderate viscosity and is suitable for forming a membrane material after being dried.
Preferably, in one of the above degradable membranes, the mass ratio of the chitosan, the sodium carboxymethyl cellulose, the low-temperature co-melting solvent and the distilled water in step (3) is 0.5 to 1: 0.05-0.2: 0.5-1: 50, more preferably 0.5: 0.1: 1: 50.
the technical scheme has the beneficial effects that the chitosan is a cationic polysaccharide, has good film forming property, but has poor solubility, and can be dissolved in a low-acid environment. The invention dissolves chitosan in the solution containing a small amount of low-temperature co-melting solvent, can form uniform chitosan solution, and the method is simple and easy compared with the traditional method for adjusting the pH of the solvent; in addition, the sodium carboxymethyl cellulose has poor solubility but excellent film forming property, the sodium carboxymethyl cellulose and the chitosan are dissolved in the low-temperature eutectic solvent, uniform liquid can be well formed, and the sodium carboxymethyl cellulose can enhance the mechanical strength of the formed film material.
According to the technical scheme, compared with the prior art, the invention discloses the degradable film and the preparation method thereof, and the degradable film has the following beneficial effects:
the degradable film prepared by the invention is a white and transparent composite polysaccharide film, and can be degraded in water solution; the polysaccharide film has good flexibility and high mechanical strength, overcomes the defects of polysaccharide film materials in the aspect of mechanical property, and can be used as a material in a package or a slow-release carrier film material; the preparation method of the degradable film can solve the defects of high cost and poor mechanical property of the existing polysaccharide film and the defect of difficult degradation of the existing packaging film material.
Drawings
In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings used in the description of the embodiments or the prior art will be briefly described below, it is obvious that the drawings in the following description are only embodiments of the present invention, and for those skilled in the art, other drawings can be obtained according to the provided drawings without creative efforts.
FIG. 1 is a schematic drawing showing the tensile force at break and elongation of the film material of the present invention;
FIG. 2 is a schematic diagram showing the time required for dissolution of the film material of the present invention.
FIG. 3 is a Fourier infrared spectrum of the film material of the present invention.
Detailed Description
The technical solutions in the embodiments of the present invention will be clearly and completely described below, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Comparative example 1
Mixing choline chloride, glycerol and lactic acid in a ratio of 3: 2: 2 at 60 deg.c and through heating and stirring to obtain colorless transparent solution, the DES solution is the required by the present invention. 1 part of gracilaria crispata polysaccharide (with the molecular weight of 24.1kDa) is weighed, and is dissolved in 50 parts of water after 0.5 part of DES is added; adding 1 part of DES solvent into 0.5 part of chitosan and 0.1 part of sodium carboxymethylcellulose, dissolving in 50 parts of water, slowly pouring the mixture of chitosan and sodium carboxymethylcellulose into the gracilaria polysaccharide solution at 50 deg.C, and stirring to obtain uniform solution. Pouring the uniformly mixed solution into a culture dish with the diameter of 6cm and the thickness of 8-10mm, and drying at 60 ℃ to prevent the solution from forming a film.
Comparative example 2:
weighing 1 part of gracilaria crispata polysaccharide (molecular weight is 501.4kDa), adding 1 part of glycerol, and dissolving in 50 parts of water; adding 1 part of glycerol into 0.5 part of chitosan and 0.1 part of sodium carboxymethylcellulose, dissolving in 50 parts of water, slowly pouring the chitosan and sodium carboxymethylcellulose blend solution into the gracilaria polysaccharide solution at 50 ℃, and stirring the mixed solution to a uniform state. The solution after mixing was poured into a petri dish of 6cm diameter, dried at 60 ℃ to a thickness of 8-10mm, and the membrane was removed and marked as F1.
Comparative example 3
Mixing choline chloride, glycerol and lactic acid in a ratio of 3: 2: 2, heating and stirring the mixture at the temperature of 60 ℃ until a colorless transparent solution is obtained, namely the DES solution required by the invention. Weighing 1 part of sodium alginate, adding 0.5 part of DES, and dissolving in 50 parts of water; adding 1 part of DES solvent into 0.5 part of chitosan and 0.1 part of sodium carboxymethylcellulose, dissolving in 50 parts of water, slowly pouring the mixed solution of chitosan and sodium carboxymethylcellulose into the sodium alginate solution at 50 ℃, and stirring the mixed solution to a uniform state. The solution after mixing was poured into a petri dish of diameter 6cm, thickness 8-10mm, dried at 60 ℃, membrane-removed and marked as F2.
Example 1:
mixing choline chloride, glycerol and lactic acid in a ratio of 3: 2: 2, heating and stirring the mixture at the temperature of 60 ℃ until a colorless transparent solution is obtained, namely the DES solution required by the invention. 1 part of gracilaria crispata polysaccharide (with the molecular weight of 298.8kDa) is weighed, and is dissolved in 50 parts of water after 0.5 part of DES is added; adding 1 part of DES solvent into 0.5 part of chitosan and 0.1 part of sodium carboxymethylcellulose, dissolving in 50 parts of water, slowly pouring the mixture of chitosan and sodium carboxymethylcellulose into the solution of Gracilaria verrucosa at 50 deg.C, and stirring to obtain uniform mixture. The solution after mixing was poured into a petri dish of diameter 6cm, thickness 8-10mm, dried at 60 ℃, membrane-removed and marked as F3.
Example 2:
choline chloride, glycerol and lactic acid are heated and stirred at 60 ℃ to form a colorless transparent solution, namely the DES solution required by the invention. Weighing 1 part of gracilaria crispatus polysaccharide (molecular weight is 501.4kDa), adding 0.5 part of DES, and dissolving in 50 parts of water; adding 1 part of DES solvent into 0.5 part of chitosan and 0.1 part of sodium carboxymethylcellulose, dissolving in 50 parts of water, slowly pouring the mixture of chitosan and sodium carboxymethylcellulose into the solution of Gracilaria gracilaria at 50 deg.C, stirring and mixing to obtain uniform solution. The solution after mixing was poured into a petri dish of diameter 6cm, thickness 8-10mm, dried at 60 ℃, membrane-removed and marked as F4.
The invention tests the mechanical properties and degradability of the film materials prepared in comparative examples 1-3 and examples 1-2.
Determination of tensile force at break and elongation of film Material
The mechanical properties of the membrane material were evaluated for tensile strength and elongation at break using a TA-XT Pluc-C texture analyser (Stable Micro Systems, TA-XT PlusC, UK). The films were prepared as identically sized sheets (90 mm. times.15 mm). The distance between the initial grips and the stretching speed of the grips were set to 60mm and 5mm/s, respectively. Tensile strength (MPa) (f (n))/(thickness × (mm)), elongation at break (%) (. DELTA.L/L)0. The resulting breaking tensile force and elongation were measured and are shown in FIG. 1.
As shown in fig. 1, film F1 using glycerol as plasticizer has a breaking tensile force significantly lower than F2, F3 and F4 with DES as plasticizer. The tensile strength of the F2 taking sodium alginate as the main raw material is obviously lower than that of the F3 and F4 taking the gracilaria polysaccharide as the raw material. In comparative example 1, the gracilaria polysaccharide with molecular weight of 24.1kDa could not form membrane material, while those used in F3 and F4, which have molecular weights of 298.8kDa and 501.4kDa respectively, have good membrane forming property, and the tensile strength of F4 is significantly better than that of F3, indicating that the molecular weight of the gracilaria polysaccharide has an influence on the membrane forming property. The elongation at break of F4 is significantly reduced compared with F1, F2 and F3, which indicates that the gracilaria polysaccharide with too high molecular weight can cause the elongation of the membrane material to be reduced, and the molecular weight of the gracilaria polysaccharide used in the membrane-forming material can be controlled according to the actual requirement. The larger the molecular weight, the greater the tensile strength of the formed membrane material, but with the increase of the molecular weight, the corresponding elongation at break is reduced, and the molecular weight is between 200kDa and 550 kDa.
Determination of the degradability of the Membrane Material
The membrane material was placed in a container containing 20mL of distilled water and stirred at 25 ℃. The time required for complete dissolution of the membrane material was observed. The time required for dissolution of the membrane material is shown in figure 2.
As can be seen from fig. 2, the film material F1, in which glycerol was used as a plasticizer, was more easily degraded, which may be related to intermolecular binding force. The degradation times of F2, F3 and F4 are all significantly higher than that of F1, indicating that the intermolecular binding of polysaccharides is tighter, and DES makes the structure of the membrane material more complex, and therefore takes longer to degrade.
FIG. 3 is Fourier infrared spectrum of sodium carboxymethylcellulose, chitosan, gracilaria crispatus polysaccharide (or sodium alginate) and their blended film. The gracilaria crispatus polysaccharide is 3419cm-1Absorption of C-H stretching vibration, infrared spectrum of 3406cm of sodium carboxymethylcellulose-1The absorption peak is the stretching vibration of O-H, 2929cm-1The left and right sides absorb C-H telescopic vibration, 1126cm-1The absorption peaks of (A) are C-O stretching vibration and O-H bending vibration, respectively. In the infrared spectrum of chitosan, 3448cm-1The position is a stretching vibration multiple absorption peak of O-H and N-H forming hydrogen bond association, 1650cm-1Corresponds to the stretching vibration absorption peak of the chitosan amide I band, and 1494cm-1Corresponds to the shock absorption peak of the amide II band. In the infrared spectrum of the blended film, at 1652cm-1And 1592cm-1The vibration absorption peaks of the amide I band and the amide II band respectively appear, which proves that the surface of the sodium carboxymethyl cellulose film is successfully coated with chitosan. In addition, it can be seen from the infrared spectrum that the absorption peak of O-H stretching vibration is broadened and shifted to the low wavenumber region, mainly because the formation of hydrogen bonding lowers the chemical bond force constant of the hydroxyl group participating in hydrogen bonding, and the absorption frequency is shifted to the low wavenumber direction.
The embodiments in the present description are described in a progressive manner, each embodiment focuses on differences from other embodiments, and the same and similar parts among the embodiments are referred to each other. For the scheme disclosed by the embodiment, the scheme corresponds to the method disclosed by the embodiment, so that the description is simple, and the relevant points can be referred to the method part for description.
The previous description of the disclosed embodiments is provided to enable any person skilled in the art to make or use the present invention. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments without departing from the spirit or scope of the invention. Thus, the present invention is not intended to be limited to the embodiments shown herein but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.
Claims (7)
1. The degradable film is characterized by comprising the following raw materials in parts by weight: 1-2 parts of gracilaria crispa polysaccharide, 0.2-0.5 part of chitosan, 0.05-0.1 part of sodium carboxymethylcellulose, 0.5-3 parts of low-temperature co-melting solvent and 98-110 parts of distilled water;
the low-temperature co-melting solvent is prepared from choline chloride, glycerol and lactic acid in a mass ratio of (1-3) to (0.5-2);
the molecular weight of the gracilaria fragile polysaccharide is more than 200kDa and less than 550 kDa.
2. A method of preparing the degradable film of claim 1, comprising the steps of: the method comprises the steps of taking gracilaria crispa polysaccharide, chitosan and sodium carboxymethylcellulose as raw materials, taking a low-temperature co-melting solvent formed by choline chloride, glycerol and lactic acid as a dissolution promoter and a plasticizer, taking distilled water as a solvent, heating and stirring until the solution is colorless and transparent, pouring the solution into a container, drying, and uncovering the film to obtain the degradable film.
3. The method of claim 2, comprising the steps of:
(1) weighing choline chloride, glycerol and lactic acid, and stirring under heating condition to obtain colorless transparent liquid, namely the low-temperature co-melting solvent;
(2) adding a small amount of low-temperature co-melting solvent into the fragile gracilaria polysaccharide, and dissolving in distilled water to obtain a fragile gracilaria solution;
(3) adding a small amount of low-temperature co-melting solvent into chitosan and sodium carboxymethyl cellulose, and dissolving in distilled water to obtain a chitosan and sodium carboxymethyl cellulose blending solution;
(4) pouring the chitosan and sodium carboxymethylcellulose blend into the gracilaria solution, stirring and mixing under heating to uniform state, then pouring into a container, drying, and uncovering the film to obtain the degradable film.
4. The production method according to claim 2 or 3, wherein the heating temperature is 50 to 80 ℃.
5. The method according to claim 2 or 3, wherein the drying is carried out by drying in a forced air dryer at 40-70 ℃ for 6-10 hours until film formation.
6. The preparation method according to claim 3, wherein the mass ratio of the fragile gracilaria polysaccharide, the low-temperature co-melting solvent and the distilled water in step (2) is 1-2: 0.5: 50.
7. the preparation method according to claim 3, wherein the mass ratio of the chitosan, the sodium carboxymethyl cellulose, the low-temperature co-melting solvent and the distilled water in the step (3) is 0.5: 0.05-0.1: 1: 50.
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH10279597A (en) * | 1998-05-06 | 1998-10-20 | Suzuyo Kk | Seaweed lectin and its production |
CN102633894A (en) * | 2012-04-16 | 2012-08-15 | 中国科学院宁波材料技术与工程研究所 | Method for preparing high-concentration large-sized seaweed biomass solution and polysaccharide extract |
CN103405775A (en) * | 2013-07-30 | 2013-11-27 | 浙江工业大学 | Hollow gracilaria polysaccharide capsule and preparation method thereof |
CN104987543A (en) * | 2015-07-31 | 2015-10-21 | 云南中烟工业有限责任公司 | Preparation method and application of ternary blend polysaccharide containing konjak glucomannan, chitosan and sodium carboxymethylcellulose |
CN110183739A (en) * | 2019-05-28 | 2019-08-30 | 天津科技大学 | A kind of degradable scleroglucan natural complex fresh-keeping film and the preparation method and application thereof |
-
2021
- 2021-02-03 CN CN202110166152.9A patent/CN112812379B/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH10279597A (en) * | 1998-05-06 | 1998-10-20 | Suzuyo Kk | Seaweed lectin and its production |
CN102633894A (en) * | 2012-04-16 | 2012-08-15 | 中国科学院宁波材料技术与工程研究所 | Method for preparing high-concentration large-sized seaweed biomass solution and polysaccharide extract |
CN103405775A (en) * | 2013-07-30 | 2013-11-27 | 浙江工业大学 | Hollow gracilaria polysaccharide capsule and preparation method thereof |
CN104987543A (en) * | 2015-07-31 | 2015-10-21 | 云南中烟工业有限责任公司 | Preparation method and application of ternary blend polysaccharide containing konjak glucomannan, chitosan and sodium carboxymethylcellulose |
CN110183739A (en) * | 2019-05-28 | 2019-08-30 | 天津科技大学 | A kind of degradable scleroglucan natural complex fresh-keeping film and the preparation method and application thereof |
Non-Patent Citations (4)
Title |
---|
C.Y. Wong等.Effect of deep eutectic solvent in proton conduction and thermal behaviour of chitosan-based membrane.《Journal of Molecular Liquids》.2018,第269卷第675–683页. * |
CMC可食性复合膜的研制;陈维新;《广州食品工业科技》;20040930;第20卷(第3期);第80-82、106页 * |
Effect of deep eutectic solvent in proton conduction and thermal behaviour of chitosan-based membrane;C.Y. Wong等;《Journal of Molecular Liquids》;20180820;第269卷;第675–683页 * |
Plasticizing of chitosan films with deep eutectic mixture of malonic acid and choline chloride;Maria P. Sokolova等;《Carbohydrate Polymers》;20180613;第197卷;第548–557页 * |
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